EP1840124B1 - Sel d'ammonium quaternaire, electrolyte, solution electrolytique et dispositif electrochimique - Google Patents

Sel d'ammonium quaternaire, electrolyte, solution electrolytique et dispositif electrochimique Download PDF

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EP1840124B1
EP1840124B1 EP06700857A EP06700857A EP1840124B1 EP 1840124 B1 EP1840124 B1 EP 1840124B1 EP 06700857 A EP06700857 A EP 06700857A EP 06700857 A EP06700857 A EP 06700857A EP 1840124 B1 EP1840124 B1 EP 1840124B1
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formula
quaternary ammonium
chain
ammonium salt
carbonate
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EP1840124A1 (fr
EP1840124A4 (fr
Inventor
Tetsuo Nishida
Kazutaka Hirano
Megumi Tomisaki
Akihiro Nabeshima
Yoshinobu Abe
Hiroaki Tokuda
Akinori Oka
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Otsuka Chemical Co Ltd
Stella Chemifa Corp
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Otsuka Chemical Co Ltd
Stella Chemifa Corp
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    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D295/00—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms
    • C07D295/04—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms
    • C07D295/08—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms substituted by singly bound oxygen or sulfur atoms
    • H—ELECTRICITY
    • H01—ELECTRIC ELEMENTS
    • H01G—CAPACITORS; CAPACITORS, RECTIFIERS, DETECTORS, SWITCHING DEVICES, LIGHT-SENSITIVE OR TEMPERATURE-SENSITIVE DEVICES OF THE ELECTROLYTIC TYPE
    • H01G11/00—Hybrid capacitors, i.e. capacitors having different positive and negative electrodes; Electric double-layer [EDL] capacitors; Processes for the manufacture thereof or of parts thereof
    • H01G11/54—Electrolytes
    • H01G11/58—Liquid electrolytes
    • H01G11/62—Liquid electrolytes characterised by the solute, e.g. salts, anions or cations therein
    • H—ELECTRICITY
    • H01—ELECTRIC ELEMENTS
    • H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M10/00—Secondary cells; Manufacture thereof
    • H01M10/05—Accumulators with non-aqueous electrolyte
    • H01M10/056—Accumulators with non-aqueous electrolyte characterised by the materials used as electrolytes, e.g. mixed inorganic/organic electrolytes
    • H—ELECTRICITY
    • H01—ELECTRIC ELEMENTS
    • H01G—CAPACITORS; CAPACITORS, RECTIFIERS, DETECTORS, SWITCHING DEVICES, LIGHT-SENSITIVE OR TEMPERATURE-SENSITIVE DEVICES OF THE ELECTROLYTIC TYPE
    • H01G11/00—Hybrid capacitors, i.e. capacitors having different positive and negative electrodes; Electric double-layer [EDL] capacitors; Processes for the manufacture thereof or of parts thereof
    • H01G11/54—Electrolytes
    • H01G11/58—Liquid electrolytes
    • H01G11/60—Liquid electrolytes characterised by the solvent
    • H—ELECTRICITY
    • H01—ELECTRIC ELEMENTS
    • H01G—CAPACITORS; CAPACITORS, RECTIFIERS, DETECTORS, SWITCHING DEVICES, LIGHT-SENSITIVE OR TEMPERATURE-SENSITIVE DEVICES OF THE ELECTROLYTIC TYPE
    • H01G9/00—Electrolytic capacitors, rectifiers, detectors, switching devices, light-sensitive or temperature-sensitive devices; Processes of their manufacture
    • H01G9/20—Light-sensitive devices
    • H01G9/2004—Light-sensitive devices characterised by the electrolyte, e.g. comprising an organic electrolyte
    • H01G9/2013—Light-sensitive devices characterised by the electrolyte, e.g. comprising an organic electrolyte the electrolyte comprising ionic liquids, e.g. alkyl imidazolium iodide
    • H—ELECTRICITY
    • H01—ELECTRIC ELEMENTS
    • H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M2300/00—Electrolytes
    • H01M2300/0017—Non-aqueous electrolytes
    • H01M2300/0025—Organic electrolyte
    • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02E—REDUCTION OF GREENHOUSE GAS [GHG] EMISSIONS, RELATED TO ENERGY GENERATION, TRANSMISSION OR DISTRIBUTION
    • Y02E10/00—Energy generation through renewable energy sources
    • Y02E10/50—Photovoltaic [PV] energy
    • Y02E10/542—Dye sensitized solar cells
    • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02E—REDUCTION OF GREENHOUSE GAS [GHG] EMISSIONS, RELATED TO ENERGY GENERATION, TRANSMISSION OR DISTRIBUTION
    • Y02E60/00—Enabling technologies; Technologies with a potential or indirect contribution to GHG emissions mitigation
    • Y02E60/10—Energy storage using batteries
    • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02E—REDUCTION OF GREENHOUSE GAS [GHG] EMISSIONS, RELATED TO ENERGY GENERATION, TRANSMISSION OR DISTRIBUTION
    • Y02E60/00—Enabling technologies; Technologies with a potential or indirect contribution to GHG emissions mitigation
    • Y02E60/13—Energy storage using capacitors
    • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
    • Y02P70/00—Climate change mitigation technologies in the production process for final industrial or consumer products
    • Y02P70/50—Manufacturing or production processes characterised by the final manufactured product

Definitions

  • the present invention relates to quaternary ammonium salts, electrolytes, electrolytic solutions and electrochemical devices. More particularly, the invention relates to functional materials which are usable as electrolytes having a high solubility in organic solvents, high electrical conductivity and small in environmental load.
  • the electrical conductivity of nonaqueous electrolytic solutions comprising such a solid electrolyte dissolved in a solvent varies with the concentration of the electrolyte. With a rise in the concentration, the ion concentration of the solution increases to increase the electrical conductivity, which will reach a maximum in due course. The electrical conductivity reaching the maximum starts to decrease presumably because the electrolyte becomes difficult to dissociate and increases in viscosity at the same time owing to increased interaction between the solvent and ions and between the ions as the number of ions increases in the electrolytic solution. When further increasing in concentration, the electrolyte becomes no longer dissociable, and the concentration of the electrolyte is saturated.
  • salts having a melting point around room temperature or salts having a melting point not higher than room temperature are salts having a melting point around room temperature or salts having a melting point not higher than room temperature (salts melting at room temperature). It is known that even if solid at room temperature, such salts dissolve in organic solvents at a higher concentration than usual electrolytes. Furthermore, the salts melting at room temperature are miscible with a specific organic solvent in a desired ratio. Accordingly, these salts afford electrolytic solutions having a high concentration not available by dissolving conventional solid electrolytes in organic solvents, while although having a high concentration, the solution is less likely to encounter the problem that the salt will separate out in a low-temperature environment. The salt melting at room temperature is itself liquid and is therefore usable singly as an electrolyte.
  • Fluoric anions especially include many which have the drawback of hydrolyzing in the presence of water to produce highly toxic hydrogen fluoride.
  • An object of the present invention is to provide an electrolyte which is highly soluble in organic solvents, highly reliable at low temperatures, highly electrically conductive and less likely to burden the environment, and further to provide electrochemical device having such advantages.
  • EP-A-1512460 which is a document pursuant to Art. 54 (3) EPC describes a method for preparing ionic liquids of general formula [X + ][SCN - ] wherein [X + ] is a hydrophilic or hydrophobic cation.
  • EP-A-1365427 relates to an electric double layer capacitor in which an electrolyte is used which generally includes a fluorinated anion.
  • the electrolyte may include a pyrrolidinium salt.
  • JP-A-10055717 describes a pyridinium based ionic compound as an electrolyte.
  • EP-A-1642894 which is a document pursuant to Art. 54 (3) EPC is related to a quaternary ammonium salt including a fluorine-containing anion, and an electrolytic solution and an electrochemical device using the salt.
  • EP-A-1698631 which is a document pursuant to Art. 54 (3) EPC is related to ionic liquids comprising at least an organic ammonium ion and at least a fluorinated anion.
  • the present invention provides the following items.
  • the present invention provides a quaternary ammonium salt of the formula (1), and an electrolytic solution containing the salt wherein R 1 is straight-chain or branched alkyl having 1 to 4 carbon atoms, R 2 is straight-chain or branched alkyl having 1 to 3 carbon atoms, and X - is N(CN) 2 - or SCN - .
  • Examples of straight-chain or branched alkyl having 1 to 4 carbon atoms represented by R 1 are methyl, ethyl, n-propyl, iso-propyl, n-butyl, sec-butyl and tert-butyl.
  • Preferable are straight-chain or branched alkyl having 1 to 3 carbon atoms. More preferable are methyl and ethyl.
  • Examples of straight-chain or branched alkyl having 1 to 3 carbon atoms represented by R 2 are methyl, ethyl, n-propyl and iso-propyl, Preferable are methyl and ethyl.
  • Examples of quaternary ammonium salts of the present invention are N-methoxymethyl-N-methylpyrrolidinium dicyanamide, N-ethyl-N-methoxymethylpyrrolidinium dicyanamide, N-methoxymethyl-N-n-propylpyrrolidinium dicyanamide, N-methoxymethyl-N-iso-propylpyrrolidinium dicyanamide, N-n-butyl-N-methoxymethylpyrrolidinium dicyanamide, N-iso-butyl-N-methoxymethylpyrrolidinium dicyanamide, N-tert-butyl-N-methoxymethylpyrrolidinium dicyanamide, N-methoxymethyl-N-methylpyrrolidinium thiocyanate, N-ethyl-N-methoxymethylpyrrolidinium thiocyanate, N-methoxymethyl-N-n-propylpyrrolidinium thiocyanate, N-methoxymethyl-N-
  • N-methoxymethyl-N-methylpyrrolidinium dicyanamide N-ethyl-N-methoxymethylpyrrolidinium dicyanamide, N-ethoxymethyl-N-methylpyrrolidinium dicyanamide and N-ethoxymethyl-N-ethylpyrrolidinium dicyanamide.
  • N-methoxymethyl-N-methylpyrrolidinium thiocyanate Preferable are N-methoxymethyl-N-methylpyrrolidinium thiocyanate, N-ethyl-N-methoxymethylpyrrolidinium thiocyanate, N-ethoxymethyl-N-methylpyrrolidinium thiocyanate and N-ethoxymethyl-N-ethylpyrrolidinium thiocyanate.
  • N-methoxymethyl-N-methylpyrrolidinium thiocyanate More preferable are N-methoxymethyl-N-methylpyrrolidinium thiocyanate and N-ethoxymethyl-N-methylpyrrolidinium thiocyanate.
  • the quaternary ammonium salt of the present invention can be prepared by various processes. Typical of these processes are represented by Equation-1 and Equation-2 given below.
  • An alkylpyrrolidine of the formula (5) wherein R 1 is the same as above is reacted with a compound of the formula (6) wherein R 2 is the same as above, and Y is Cl, Br, I or the like to prepare a quaternary ammonium salt of the formula (1a), which is then subjected to salt-exchange reaction with a compound of the formula (7) to prepare a quaternary ammonium salt of the formula (1).
  • M in the formula (7) is one of atoms including hydrogen, alkali metal atoms such as Na, K and Li, alkaline earth metal atoms such as Ca, Mg and Ba, and metal atoms such as Ag.
  • tertiary amine of the formula (5) serving as the starting material and the compound of the formula (6) are both known substances.
  • Examples of tertiary amine of the formula (5) are methylpyrrolidine, ethylpyrrolidine, n-propylpyrrolidine, isopropylpyrrolidine, n-butylpyrrolidine, isobutylpyrrolidine, tert-butylpyrrolidine, etc.
  • Examples of compounds of the formula (6) are chloromethyl methyl ether, bromomethyl methyl ether, iodomethyl methyl ether, chloromethyl ethyl ether, bromomethyl ethyl ether, iodomethyl ethyl ether, chloromethyl n-propyl ether, bromomethyl n-propyl ether, iodomethyl n-propyl ether, chloromethyl iso-propyl ether, bromomethyl iso-propyl ether, iodomethyl iso-propyl ether, etc.
  • the tertiary amine of the formula (5) and the compound of the formula (6) are reacted in a suitable solvent.
  • the solvent to be used can be a wide variety of known solvents insofar as they are capable of solving the tertiary amine of the formula (5) and the compound of the formula (6) and will not adversely affect the reaction.
  • solvents are benzene, toluene, xylene and like aromatic hydrocarbons, dichloromethane, chloroform, carbon tetrachloride and like hydrocarbon halides, methanol, ethanol, isopropanol, n-butanol, tert-butanol and like lower alcohols, acetone, methyl ethyl ketone and like ketones, diethyl ether, diisopropyl ether and like ethers, methyl acetate, ethyl acetate, butyl acetate and like esters, n-hexane, n-heptane and like aliphatic hydrocarbons, cyclohexane and like aliphatic hydrocarbons, etc.
  • solvents Preferable among these solvents are toluene and like aromatic hydrocarbons, chloroform and like hydrocarbon halides, acetone and like ketones and methyl acetate and like esters. These solvents can be used singly, or at least two of them are usable in admixture. Preferable to use are solvents which are free from water (up to 1000 ppm in water content).
  • the tertiary amine of the formula (5) and the compound of the formula (6) are used in the ratio usually of 0.5 to 5 moles, preferably 0.9 to 1.2 moles, of the latter per mole of the former.
  • the reaction is carried out usually at -30 to 100° C, more particularly at -10 to 40° C.
  • the reaction is completed generally in several hours to about 24 hours.
  • reaction of the quaternary ammonium salt of the formula (1a) obtained above with the compound of the formula (7) is carried out by a usual salt exchange reaction.
  • the compound of the formula (7) used as a starting material is a known compound. Examples of these are HN(CN) 2 , LiN(CN) 2 , NaN(CN) 2 , KN(CN) 2 , AgN(CN) 2 , HSCN, LiSCN, NaSCN, KSCN, and AgSCN.
  • This salt exchange reaction is carried out in a suitable solvent.
  • the solvent to be used can be a wide variety of known solvents insofar as they are capable of dissolving the quaternary ammonium salt of the formula (1a) and the compound of the formula (7) and will not adversely affect the reaction.
  • the alkoxypyrrolidine of the formula (8) serving as the starting material and the compound of the formula (9) are both known substances.
  • the quaternary ammonium salt of the formula (1a) and the compound of the formula (7) are used in the ratio usually of 0.3 to 5 moles, preferably 0.9 to 1.2 moles, of the latter per mole of the former.
  • the reaction proceeds usually rapidly, so that a solution of the two reactants in a solvent is reacted at about 5 to about 150° C for about 10 minutes to about 24 hours.
  • Activated carbon materials are desirable as carbon materials. Examples of such materials are sawdust activated carbon, coconut shell activated carbon, pitch or coke activated carbon, phenolic resin activated carbon, polyacrylonitrile activated carbon, celluosic activated carbon, etc.
  • the separator has high electron insulating properties, is highly wettable with the electrolytic solution and highly permeable to ions, and needs to be electrochemically stable within the range of voltages to be applied.
  • the material for the separator is not limited particularly, it is suitable to use paper made from rayon, Manila hemp or the like, porous polyolefin film, nonwoven polyethylene fabric, nonwoven polypropylene fabric, etc.
  • compositions were each placed into glass containers having a screw plug inside the dry box, in an amount of 4 cc in each container and brought out of the dry box.
  • the glass containers containing the composition were immersed in a constant-temperature bath and held at 25°C, 0°C or -30°C for 5 hours and checked for state visually.
  • the results are shown in Tables, in which "-" indicates separation into two layers, and "solid” represents a solid state.
  • Example 2 electrolyte AN electrical conductivity (25°C) (0°C) (-30°C) (wt%) (wt%) (mS/cm) (mS/cm) (mS/cm) 20 80 50.4 44.3 29.6 Ex. 6 40 60 68.8 51.4 32.9 50 50 70.0 53.5 32.1 60 40 67.2 49.4 27.4 80 20 48.1 30.3 14.1 100 0 21.6 10.2 2.7
  • N-methylpyrrolidine (31.10 g, reagent, product of Tokyo Kasei Co., Ltd.) was dissolved in 124.30 g of toluene, followed by replacement with nitrogen.
  • To the solution was added dropwise 61.22 g of bromoethyl methyl ether (reagent, product of Aldrich Corp.) at 27°C over a period of 1 hour.
  • the mixture was heated to a gradually raised temperature and then stirred at 60 to 70°C for 37 hours to terminate the reaction.
  • the reaction mixture was cooled to room temperature, and the resulting solids were filtered off under a nitrogen stream.

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  • Electric Double-Layer Capacitors Or The Like (AREA)
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  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Electrolytic Production Of Non-Metals, Compounds, Apparatuses Therefor (AREA)

Abstract

L'invention concerne un sel d'ammonium quaternaire représenté par la formule (1), une solution électrolytique et un dispositif électrochimique. Dans la formule (1), R1 représente une chaîne droite ou un groupe alkyle ramifié présentant de 1 à 4 atomes de carbone, R2 représente une chaîne droite ou un groupe alkyle ramifié présentant de 1 à 3 atomes de carbone, et X-1 représente N(CN)2-, SCN-, NO3-, NCO- ou NO2-).

Claims (15)

  1. Sel d'ammonium quaternaire de formule (1)
    Figure imgb0021
     dans laquelle R1 est un groupe alkyle à chaîne linéaire ou ramifiée ayant de 1 à 4 atomes de carbone, R2 est un groupe alkyle à chaîne linéaire ou ramifiée ayant de 1 à 3 atomes de carbone, et X- est N(CN)2 - ou SCN-.
  2. Sel d'ammonium quaternaire de formule (2)
    Figure imgb0022
     dans laquelle X- est tel que défini ci-dessus, et Me est un groupe méthyle.
  3. Composition qui comprend au moins l'un des sels d'ammonium quaternaire selon l'une quelconque des revendications 1 et 2 et d'un solvant organique.
  4. Composition selon la revendication 3, dans laquelle le solvant organique est au moins un choisi parmi les esters cycliques de l'acide carbonique, les esters à chaîne de l'acide carbonique, les esters de l'acide phosphorique, les éthers cycliques, les éthers à chaîne, les composés lactone, les esters à chaîne, les composés nitrile, les composés amide et les composés sulfone.
  5. Composition selon la revendication 4, dans laquelle le solvant organique est au moins un choisi parmi le carbonate d'éthylène, le carbonate de propylène, le carbonate de diméthyle, le carbonate d'éthylméthyle, le diméthoxyéthane et l'acétonitrile.
  6. Composition selon la revendication 4, dans laquelle le solvant organique est au moins un choisi parmi le carbonate de propylène et l'acétonitrile.
  7. Electrolyte de formule (3)
    Figure imgb0023
     dans laquelle R1 est un groupe alkyle à chaîne linéaire ou ramifiée ayant de 1 à 4 atomes de carbone, R2 est un groupe alkyle à chaîne linéaire ou ramifiée ayant de 1 à 3 atomes de carbone, et X- est N(CN)2 - ou SCN-.
  8. Electrolyte de formule (4)
    Figure imgb0024
     dans laquelle X- est tel que défini ci-dessus, et Me est un groupe méthyle.
  9. Solution électrolytique, la solution comprenant au moins l'un des sels d'ammonium quaternaire selon l'une quelconque des revendications 7 et 8.
  10. Solution électrolytique qui comprend au moins l'un des sels d'ammonium quaternaire selon l'une quelconque des revendications 7 et 8 et d'un solvant organique.
  11. Solution électrolytique selon la revendication 10, dans laquelle le solvant organique est au moins un choisi parmi les esters cycliques de l'acide carbonique, les esters à chaîne de l'acide carbonique, les esters de l'acide phosphorique, les éthers cycliques, les éthers à chaîne, les composés lactone, les esters à chaîne, les composés nitrile, les composés amide et les composés sulfone.
  12. Solution électrolytique selon la revendication 11, dans laquelle le solvant organique est au moins un choisi parmi le carbonate d'éthylène, le carbonate de propylène, le carbonate de diméthyle, le carbonate d'éthylméthyle, le diméthoxyéthane et l'acétonitrile.
  13. Solution électrolytique selon la revendication 11, dans laquelle le solvant organique est au moins un choisi parmi le carbonate de propylène et l'acétonitrile.
  14. Dispositif électrochimique utilisant la solution électrolytique de l'une quelconque des revendications 9 à 13.
  15. Procédé de préparation d'un sel d'ammonium quaternaire de formule (1) qui comprend :
    (a) une étape consistant à faire réagir une alkylpyrrolidine de formule (5) et un composé de formule (6) pour préparer un sel d'ammonium quaternaire de formule (1a)
    Figure imgb0025
     dans laquelle R1 est un groupe alkyle à chaîne linéaire ou ramifiée ayant de 1 à 4 atomes de carbone,
    Figure imgb0026
     dans laquelle R2 est un groupe alkyle à chaîne linéaire ou ramifiée ayant de 1 à 3 atomes de carbone et Y est Cl, Br ou I,
    Figure imgb0027
     dans laquelle R1, R2 et Y sont tels que définis ci-dessus, et
    (b) une étape consistant à faire réagir le sel d'ammonium quaternaire de formule (1a) et un composé de formule (7)

            MX     (7)

    dans laquelle M est un atome d'hydrogène, un atome de métal alcalin, un atome de métal alcalino-terreux ou un atome de métal, et X- est N(CN)2 - ou SCN-.
EP06700857A 2005-01-12 2006-01-12 Sel d'ammonium quaternaire, electrolyte, solution electrolytique et dispositif electrochimique Expired - Lifetime EP1840124B1 (fr)

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JP2005005580 2005-01-12
PCT/JP2006/300668 WO2006077895A1 (fr) 2005-01-12 2006-01-12 Sel d'ammonium quaternaire, electrolyte, solution electrolytique et dispositif electrochimique

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EP1840124A1 EP1840124A1 (fr) 2007-10-03
EP1840124A4 EP1840124A4 (fr) 2009-04-01
EP1840124B1 true EP1840124B1 (fr) 2010-03-17

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US (1) US7854854B2 (fr)
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JP (1) JP4802108B2 (fr)
DE (1) DE602006012933D1 (fr)
WO (1) WO2006077895A1 (fr)

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JP5027997B2 (ja) * 2005-05-17 2012-09-19 株式会社日本触媒 導電性付与剤及び導電性材料
CA2726143A1 (fr) * 2008-05-29 2009-12-10 Leyden Energy, Inc. Cellules electrochimiques avec electrolyte liquide ionique
JP5473296B2 (ja) * 2008-11-04 2014-04-16 大塚化学株式会社 第４級アンモニウム塩
JP2010192226A (ja) * 2009-02-18 2010-09-02 Toyo Ink Mfg Co Ltd 電解質、電解質組成物、およびそれらの応用
CN102379059A (zh) * 2009-04-30 2012-03-14 横滨橡胶株式会社 光电转换元件用电解质、以及使用了该电解质的光电转换元件和染料敏化太阳能电池
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EP1840124A4 (fr) 2009-04-01
US20100038578A1 (en) 2010-02-18
DE602006012933D1 (de) 2010-04-29
WO2006077895A1 (fr) 2006-07-27
JPWO2006077895A1 (ja) 2008-08-07

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